Variant report

Variant	nsv1028369
Chromosome Location	chr7:124967804-125508233
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1674)
CpG islands
(count:0)
Chromatin interactive
region (count:108)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1674 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:125245371-125245822	K562	blood:	n/a	n/a
2	ARID3A	chr7:125238528-125238531	K562	blood:	n/a	n/a
3	ARID3A	chr7:125145112-125145113	K562	blood:	n/a	n/a
4	ARID3A	chr7:125036847-125037232	K562	blood:	n/a	n/a
5	ARID3A	chr7:125235405-125235419	K562	blood:	n/a	n/a
6	ARID3A	chr7:125207883-125208163	K562	blood:	n/a	n/a
7	ARID3A	chr7:125112702-125112705	K562	blood:	n/a	n/a
8	ATF1	chr7:125099017-125099154	K562	blood:	n/a	n/a
9	ATF1	chr7:125036628-125037136	K562	blood:	n/a	n/a
10	ATF1	chr7:125304902-125304935	K562	blood:	n/a	n/a
11	ATF1	chr7:125102482-125102530	K562	blood:	n/a	n/a
12	ATF1	chr7:125155568-125155672	K562	blood:	n/a	n/a
13	ATF2	chr7:125292085-125292579	GM12878	blood:	n/a	n/a
14	ATF2	chr7:124995766-124996416	GM12878	blood:	n/a	n/a
15	ATF2	chr7:125208736-125209317	GM12878	blood:	n/a	n/a
16	ATF2	chr7:124995927-124996331	GM12878	blood:	n/a	n/a
17	ATF2	chr7:125208800-125209277	GM12878	blood:	n/a	n/a
18	ATF3	chr7:125036857-125037111	K562	blood:	n/a	n/a
19	ATF3	chr7:125245272-125245589	K562	blood:	n/a	n/a
20	BACH1	chr7:125250853-125250856	K562	blood:	n/a	n/a
21	BACH1	chr7:125144988-125145184	K562	blood:	n/a	n/a
22	BACH1	chr7:125245462-125245548	H1-hESC	embryonic stem cell:	n/a	chr7:125245471-125245485
23	BACH1	chr7:125144864-125145256	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:125432709-125432803	K562	blood:	n/a	n/a
25	BATF	chr7:125400561-125400782	GM12878	blood:	n/a	n/a
26	BATF	chr7:125444374-125444778	GM12878	blood:	n/a	n/a
27	BATF	chr7:125131056-125131238	GM12878	blood:	n/a	n/a
28	BATF	chr7:125463611-125463967	GM12878	blood:	n/a	n/a
29	BATF	chr7:124996043-124996381	GM12878	blood:	n/a	n/a
30	BATF	chr7:124996009-124996436	GM12878	blood:	n/a	n/a
31	BATF	chr7:125208879-125209269	GM12878	blood:	n/a	n/a
32	BATF	chr7:125208852-125209217	GM12878	blood:	n/a	n/a
33	BATF	chr7:125144978-125145174	GM12878	blood:	n/a	chr7:125145074-125145085
34	BCL11A	chr7:125208879-125209307	GM12878	blood:	n/a	n/a
35	BCL11A	chr7:125208927-125209202	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:125444389-125444708	GM12878	blood:	n/a	n/a
37	BCL11A	chr7:124995894-124996370	GM12878	blood:	n/a	n/a
38	BCL3	chr7:125208897-125209206	GM12878	blood:	n/a	n/a
39	BCL3	chr7:124995875-124996328	GM12878	blood:	n/a	n/a
40	BCL3	chr7:125292138-125292574	GM12878	blood:	n/a	n/a
41	BCL3	chr7:125460885-125461181	GM12878	blood:	n/a	n/a
42	BCLAF1	chr7:125208875-125209224	GM12878	blood:	n/a	n/a
43	BCLAF1	chr7:125208811-125209257	GM12878	blood:	n/a	n/a
44	BHLHE40	chr7:125178945-125179203	K562	blood:	n/a	chr7:125179077-125179098 chr7:125179081-125179094
45	BHLHE40	chr7:125208861-125209208	GM12878	blood:	n/a	n/a
46	BHLHE40	chr7:125315765-125315880	K562	blood:	n/a	n/a
47	BHLHE40	chr7:125201165-125201410	GM12878	blood:	n/a	n/a
48	BHLHE40	chr7:125242283-125242313	K562	blood:	n/a	n/a
49	BHLHE40	chr7:125052988-125053632	GM12878	blood:	n/a	n/a
50	BHLHE40	chr7:125375284-125375348	K562	blood:	n/a	n/a

No data

(count:108 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:125070959..125073239-chr7:125075739..125078658,3	K562	blood:
2	chr7:125266350..125268456-chr7:125268990..125271512,2	K562	blood:
3	chr7:125234853..125237677-chr7:125237685..125240938,4	K562	blood:
4	chr7:125003566..125005765-chr7:125027328..125029861,2	K562	blood:
5	chr7:125325822..125328394-chr7:125330208..125331998,2	K562	blood:
6	chr7:124979372..124981820-chr7:124985278..124987442,3	K562	blood:
7	chr7:125414524..125416692-chr7:125417841..125420169,2	K562	blood:
8	chr7:125449848..125452738-chr7:125466258..125468115,2	K562	blood:
9	chr3:108533640..108534622-chr7:125014752..125015433,2	MCF-7	breast:
10	chr7:125425665..125427173-chr7:125429693..125431589,2	K562	blood:
11	chr7:125269070..125270794-chr7:125275616..125278202,2	K562	blood:
12	chr7:125435373..125437398-chr7:125441806..125444028,2	K562	blood:
13	chr7:125205327..125207901-chr7:125208820..125211664,2	K562	blood:
14	chr7:125271199..125273030-chr7:125279444..125281182,2	K562	blood:
15	chr7:125458557..125461124-chr7:125464853..125467696,2	K562	blood:
16	chr7:125023517..125024026-chr7:125310752..125311652,2	MCF-7	breast:
17	chr7:125234594..125236456-chr7:125238613..125240921,2	K562	blood:
18	chr7:124699558..124701618-chr7:125055753..125057701,2	K562	blood:
19	chr7:125280203..125282931-chr7:125290069..125292178,2	K562	blood:
20	chr7:125218658..125220340-chr7:125222287..125223970,2	K562	blood:
21	chr7:125203772..125205320-chr7:125225530..125228131,2	K562	blood:
22	chr7:125241383..125243591-chr7:125245619..125247438,2	K562	blood:
23	chr7:125385605..125387936-chr7:125388625..125390972,2	K562	blood:
24	chr7:125037857..125040245-chr7:125044740..125047619,2	K562	blood:
25	chr7:125126724..125128959-chr7:125132341..125134111,2	K562	blood:
26	chr7:125480828..125483147-chr7:125484662..125486648,3	K562	blood:
27	chr7:124699671..124700472-chr7:125310284..125311293,4	MCF-7	breast:
28	chr7:125369632..125371193-chr7:125372789..125375510,2	K562	blood:
29	chr7:125226088..125228401-chr7:125230345..125233728,3	K562	blood:
30	chr7:125325822..125328394-chr7:125330208..125331998,2	K562	blood:
31	chr7:125118097..125121016-chr7:125124179..125126346,2	K562	blood:
32	chr7:124558834..124561175-chr7:124980135..124981921,2	K562	blood:
33	chr7:125014089..125016137-chr7:125017840..125020682,3	K562	blood:
34	chr7:125190321..125191930-chr7:125194449..125196273,2	K562	blood:
35	chr7:125243932..125247685-chr7:125249366..125252787,4	K562	blood:
36	chr7:125205327..125207901-chr7:125208820..125211664,2	K562	blood:
37	chr7:125385605..125387936-chr7:125388625..125390972,2	K562	blood:
38	chr7:125251686..125253446-chr7:125261235..125263882,2	K562	blood:
39	chr7:125480828..125483147-chr7:125484662..125486648,3	K562	blood:
40	chr7:125310080..125313010-chr7:125315945..125318441,2	K562	blood:
41	chr7:125414524..125416692-chr7:125417841..125420169,2	K562	blood:
42	chr7:125466756..125469484-chr9:139938867..139941802,2	MCF-7	breast:
43	chr7:125204110..125205826-chr7:125284105..125286281,2	K562	blood:
44	chr7:124846681..124848535-chr7:125206338..125208006,2	K562	blood:
45	chr7:125458557..125461124-chr7:125464853..125467696,3	K562	blood:
46	chr7:125118097..125121016-chr7:125124179..125126346,2	K562	blood:
47	chr7:125392984..125395323-chr7:125485232..125486912,2	K562	blood:
48	chr7:125241383..125243591-chr7:125245619..125247438,2	K562	blood:
49	chr7:125384743..125387377-chr7:125395816..125398229,2	K562	blood:
50	chr7:125369632..125371193-chr7:125372789..125375510,2	K562	blood:

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPAM1-5	chr7:124975307-124975469	ENSG00000237764.2
2	lnc-SPAM1-9	chr7:124985879-124986251	NONHSAT123107
3	lnc-SPAM1-5	chr7:125003489-125003570	ENSG00000237764.2
4	lnc-SPAM1-5	chr7:125019112-125019375	NONHSAT123102
5	lnc-SPAM1-6	chr7:125101535-125101704	ENSG00000227869
6	lnc-SPAM1-6	chr7:125106324-125106455	NONHSAT123109
7	lnc-SPAM1-5	chr7:124987179-124987261	ENSG00000237764.2
8	lnc-SPAM1-5	chr7:125003489-125003570	NR_110188
9	lnc-SPAM1-6	chr7:125101535-125101665	ENSG00000227869
10	lnc-SPAM1-5	chr7:124969736-124969801	NONHSAT123102
11	lnc-SPAM1-5	chr7:124970311-124970457	NONHSAT123102
12	lnc-SPAM1-6	chr7:125078165-125078351	ENSG00000227869
13	lnc-SPAM1-5	chr7:125019112-125019375	NR_110188
14	lnc-SPAM1-6	chr7:125071401-125071647	ENSG00000227869
15	lnc-SPAM1-5	chr7:124969736-124969801	NR_110188
16	lnc-SPAM1-6	chr7:125078165-125078351	NONHSAT123109
17	lnc-SPAM1-5	chr7:124969736-124969801	ENSG00000237764.2
18	lnc-SPAM1-8	chr7:124985023-124985431	NONHSAT123106
19	lnc-SPAM1-6	chr7:125078199-125078351	ENSG00000227869
20	lnc-SPAM1-5	chr7:124975307-124975469	NONHSAT123102
21	lnc-SPAM1-5	chr7:124987179-124987261	NR_110188
22	lnc-SPAM1-6	chr7:125071401-125071647	NONHSAT123109
23	lnc-SPAM1-5	chr7:125003489-125003570	NONHSAT123102
24	lnc-SPAM1-6	chr7:125101535-125101923	ENSG00000227869
25	lnc-SPAM1-6	chr7:125106324-125106455	ENSG00000227869
26	lnc-SPAM1-5	chr7:124970311-124970457	NR_110188
27	lnc-SPAM1-5	chr7:124987179-124987261	NONHSAT123102
28	lnc-SPAM1-5	chr7:125019112-125019375	ENSG00000237764.2
29	lnc-SPAM1-6	chr7:125101535-125101923	NONHSAT123109
30	lnc-SPAM1-5	chr7:124975307-124975469	NR_110188
31	lnc-SPAM1-6	chr7:125078276-125078351	ENSG00000227869
32	lnc-SPAM1-5	chr7:124970311-124970457	ENSG00000237764.2

No data

Variant related genes	Relation type
ENSG00000227869	TF binding region
ENSG00000227847	TF binding region
ENSG00000234071	TF binding region
ENSG00000107281	chromatin interactions
ENSG00000227847	chromatin interactions
ENSG00000227869	chromatin interactions
ENSG00000106302	chromatin interactions

Extended variants
information (count: 8523 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:8523 , 50 per page) page: 1 2 3 4 5 6 7 ... 171

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138688610	chr7:124967831-124967832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs17148178	chr7:124967951-124967952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146101661	chr7:124967952-124967953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553352753	chr7:124967954-124967955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73719373	chr7:124967994-124967995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568129724	chr7:124968012-124968013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527307774	chr7:124968074-124968075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187792179	chr7:124968092-124968093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531066687	chr7:124968126-124968127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544376126	chr7:124968130-124968131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201012575	chr7:124968152-124968153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139686797	chr7:124968187-124968188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530009549	chr7:124968227-124968228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546895610	chr7:124968305-124968306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566683375	chr7:124968311-124968312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192049395	chr7:124968316-124968317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551996322	chr7:124968335-124968336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573744613	chr7:124968394-124968395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149362858	chr7:124968439-124968440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12673987	chr7:124968441-124968442	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs568061665	chr7:124968563-124968564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144680164	chr7:124968595-124968596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553704877	chr7:124968664-124968665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573611398	chr7:124968665-124968666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs148574586	chr7:124968675-124968676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs60327925	chr7:124968697-124968698	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs73444706	chr7:124968821-124968822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1427583	chr7:124968901-124968902	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs561198077	chr7:124968917-124968918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145675498	chr7:124968943-124968944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540304681	chr7:124968970-124968971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs34992677	chr7:124968983-124968984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs184498119	chr7:124969000-124969001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532321976	chr7:124969094-124969095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188169542	chr7:124969121-124969122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147290964	chr7:124969122-124969123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531368719	chr7:124969187-124969188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1427582	chr7:124969215-124969216	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs192769927	chr7:124969225-124969226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184935245	chr7:124969231-124969232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550848323	chr7:124969268-124969269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189050699	chr7:124969309-124969310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569085261	chr7:124969330-124969331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547116950	chr7:124969337-124969338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs180901318	chr7:124969347-124969348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539342721	chr7:124969387-124969388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184763897	chr7:124969403-124969404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34875020	chr7:124969451-124969452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572177434	chr7:124969455-124969456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189623743	chr7:124969492-124969493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Autism	20858243	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Chordoma	21215367	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:399 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:124962000-124984400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:124974400-124974600	Enhancers	Pancreas	Pancrea
3	chr7:124975200-124977200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr7:124975200-124977600	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr7:124975400-124976800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr7:124975400-124977600	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr7:124975600-124975800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr7:124975600-124975800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr7:124975600-124976400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr7:124975600-124976600	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr7:124975600-124977400	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr7:124975800-124976600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr7:124975800-124976800	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr7:124976600-124977200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr7:124976800-124977200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr7:124977200-124978000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr7:124979000-124979200	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr7:124985800-124986400	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr7:124987000-124988200	Enhancers	HUVEC	blood vessel
20	chr7:124995000-124996000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr7:124995600-124999400	Enhancers	HUVEC	blood vessel
22	chr7:124995800-124996800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr7:124995800-124999000	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr7:124996000-124996200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr7:124996000-124996600	Enhancers	NH-A	brain
26	chr7:124996000-124997000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr7:124996400-124997600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr7:124996600-124997000	Weak transcription	NH-A	brain
29	chr7:124996800-124997800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:124997000-124997200	Enhancers	NH-A	brain
31	chr7:124997000-124999000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr7:124997200-125003800	Weak transcription	NH-A	brain
33	chr7:124997400-124999000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr7:124997600-124998400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr7:124997800-124998000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:125003800-125004400	Enhancers	NH-A	brain
37	chr7:125004800-125005000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr7:125015400-125016400	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr7:125015400-125017000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr7:125015800-125017200	Enhancers	Brain Germinal Matrix	brain
41	chr7:125021400-125023800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr7:125023800-125028000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr7:125028000-125029000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:125029000-125031000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr7:125031000-125031200	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr7:125031000-125031400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr7:125031200-125032400	Enhancers	HUVEC	blood vessel
48	chr7:125031200-125036200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr7:125032200-125032400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:125034200-125034400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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