Variant report

Variant	esv20115
Chromosome Location	chr7:98029489-98030050
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr7:98029781-98030232	A549	lung:	n/a	n/a
2	BCL3	chr7:98029764-98030361	A549	lung:	n/a	n/a
3	BCL3	chr7:98029874-98030259	GM12878	blood:	n/a	n/a
4	BHLHE40	chr7:98029995-98030226	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:98030050-98030211	K562	blood:	n/a	n/a
6	CBX3	chr7:98029872-98030832	K562	blood:	n/a	n/a
7	CCNT2	chr7:98029980-98030816	K562	blood:	n/a	n/a
8	CHD2	chr7:98029512-98030870	Hela-S3	cervix:	n/a	n/a
9	CHD2	chr7:98029855-98030718	GM12878	blood:	n/a	n/a
10	CHD2	chr7:98029911-98030239	K562	blood:	n/a	n/a
11	CHD2	chr7:98028885-98029640	GM12878	blood:	n/a	n/a
12	CREB1	chr7:98029800-98030993	HepG2	liver:	n/a	n/a
13	CTCF	chr7:98029957-98031100	A549	lung:	n/a	chr7:98030639-98030655 chr7:98030640-98030653 chr7:98030638-98030656
14	CTCF	chr7:98029945-98031379	SK-N-SH	brain:	n/a	chr7:98030639-98030655 chr7:98030640-98030653 chr7:98030638-98030656
15	CUX1	chr7:98029905-98030092	GM12878	blood:	n/a	n/a
16	E2F4	chr7:98029764-98030763	K562	blood:	n/a	chr7:98030036-98030047
17	E2F4	chr7:98029692-98029963	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F6	chr7:98029867-98030532	H1-hESC	embryonic stem cell:	n/a	chr7:98030187-98030198
19	E2F6	chr7:98029924-98030550	K562	blood:	n/a	chr7:98030187-98030198
20	E2F6	chr7:98029681-98030713	K562	blood:	n/a	chr7:98030187-98030198
21	E2F6	chr7:98029840-98030784	K562	blood:	n/a	chr7:98030187-98030198
22	E2F6	chr7:98029838-98030434	H1-hESC	embryonic stem cell:	n/a	chr7:98030187-98030198
23	E2F6	chr7:98029864-98030496	A549	lung:	n/a	chr7:98030187-98030198
24	EBF1	chr7:98029944-98030243	GM12878	blood:	n/a	n/a
25	EGR1	chr7:98029904-98030079	GM12878	blood:	n/a	chr7:98029972-98029986 chr7:98030003-98030017
26	EGR1	chr7:98029886-98030772	K562	blood:	n/a	chr7:98029972-98029986 chr7:98030531-98030545 chr7:98030003-98030017
27	ELF1	chr7:98029918-98030870	GM12878	blood:	n/a	chr7:98030095-98030107
28	ELF1	chr7:98029819-98031002	GM12878	blood:	n/a	chr7:98030095-98030107
29	ELF1	chr7:98029991-98030773	K562	blood:	n/a	chr7:98030095-98030107
30	ELF1	chr7:98029177-98029667	GM12878	blood:	n/a	n/a
31	EP300	chr7:98030000-98030879	ECC-1	luminal epithelium:	n/a	n/a
32	EP300	chr7:98029967-98030342	GM12878	blood:	n/a	n/a
33	EP300	chr7:98028689-98029686	ECC-1	luminal epithelium:	n/a	n/a
34	EP300	chr7:98030008-98030114	GM12878	blood:	n/a	n/a
35	ESR1	chr7:98029112-98029561	ECC-1	luminal epithelium:	n/a	n/a
36	ESR1	chr7:98029154-98029584	ECC-1	luminal epithelium:	n/a	n/a
37	ESR1	chr7:98029145-98029612	ECC-1	luminal epithelium:	n/a	n/a
38	ESR1	chr7:98029145-98029522	ECC-1	luminal epithelium:	n/a	n/a
39	ETS1	chr7:98029966-98030529	K562	blood:	n/a	n/a
40	FOXM1	chr7:98029805-98030205	GM12878	blood:	n/a	n/a
41	GABPA	chr7:98030010-98030910	K562	blood:	n/a	chr7:98030411-98030420 chr7:98030591-98030600
42	HDAC2	chr7:98029885-98030960	MCF-7	breast:	n/a	n/a
43	HEY1	chr7:98029865-98030449	K562	blood:	n/a	n/a
44	HEY1	chr7:98030045-98030445	K562	blood:	n/a	n/a
45	HMGN3	chr7:98030031-98030827	K562	blood:	n/a	n/a
46	MAX	chr7:98029715-98030898	A549	lung:	n/a	n/a
47	MAX	chr7:98029873-98030723	A549	lung:	n/a	n/a
48	MAX	chr7:98029894-98030825	K562	blood:	n/a	n/a
49	MAX	chr7:98030009-98030738	K562	blood:	n/a	n/a
50	MAX	chr7:98029857-98030838	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:97501305..97502999-chr7:98028998..98030520,2	K562	blood:
2	chr7:98028301..98030360-chr7:98475060..98477669,2	K562	blood:
3	chr7:98028440..98031404-chr7:98475727..98477431,2	MCF-7	breast:
4	chr7:97948534..97953392-chr7:98027922..98031084,5	MCF-7	breast:
5	chr7:98015865..98017595-chr7:98028896..98031691,2	MCF-7	breast:
6	chr7:97948846..97953573-chr7:98026962..98031463,6	MCF-7	breast:
7	chr7:97880638..97884180-chr7:98029742..98031678,3	MCF-7	breast:
8	chr7:97851992..97854043-chr7:98027877..98030619,2	K562	blood:

Variant related genes	Relation type
BAIAP2L1	TF binding region
ENSG00000196367	chromatin interactions
ENSG00000070669	chromatin interactions
ENSG00000214389	chromatin interactions
ENSG00000272950	chromatin interactions
ENSG00000205356	chromatin interactions
ENSG00000164713	chromatin interactions

Extended variants
information (count: 38 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:38 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568774379	chr7:98029501-98029502	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs192719549	chr7:98029531-98029532	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs10254734	chr7:98029545-98029546	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs566858080	chr7:98029552-98029553	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs113835051	chr7:98029563-98029564	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs142592162	chr7:98029574-98029575	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs184206600	chr7:98029606-98029607	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs567862246	chr7:98029631-98029632	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs13307080	chr7:98029636-98029637	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs13307229	chr7:98029639-98029640	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs13307082	chr7:98029651-98029652	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs370695848	chr7:98029663-98029664	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs372982677	chr7:98029668-98029669	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs143779666	chr7:98029675-98029676	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs202113691	chr7:98029680-98029681	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs118065856	chr7:98029686-98029687	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	mRNA abundance
17	rs141163580	chr7:98029697-98029698	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs13307091	chr7:98029705-98029706	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs188909348	chr7:98029707-98029708	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs13307237	chr7:98029710-98029711	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs200460094	chr7:98029720-98029721	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs538414264	chr7:98029731-98029732	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs556912413	chr7:98029746-98029747	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs578256753	chr7:98029808-98029809	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs13307284	chr7:98029811-98029812	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs545679425	chr7:98029829-98029830	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs377379838	chr7:98029838-98029839	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs111155372	chr7:98029841-98029842	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs548771774	chr7:98029864-98029865	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs572757699	chr7:98029879-98029880	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs370800355	chr7:98029937-98029938	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs192292427	chr7:98029946-98029947	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs561416726	chr7:98029951-98029952	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs529067096	chr7:98029973-98029974	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs544039019	chr7:98029996-98029997	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs562322341	chr7:98029997-98029998	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs533107111	chr7:98030004-98030005	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs75133638	chr7:98030026-98030027	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:176 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:98027600-98029600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr7:98027600-98030600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr7:98027800-98030400	Active TSS	Fetal Intestine Small	intestine
4	chr7:98027800-98030400	Active TSS	Rectal Mucosa Donor 29	rectum
5	chr7:98027800-98030400	Active TSS	Stomach Mucosa	stomach
6	chr7:98027800-98030800	Active TSS	iPS-20b Cell Line	embryonic stem cell
7	chr7:98027800-98031000	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr7:98028000-98030000	Active TSS	Colonic Mucosa	Colon
9	chr7:98028000-98031000	Active TSS	Rectal Smooth Muscle	rectum
10	chr7:98028400-98030000	Active TSS	Fetal Intestine Large	intestine
11	chr7:98028400-98030600	Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr7:98028400-98030600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr7:98028400-98030600	Active TSS	Duodenum Mucosa	Duodenum
14	chr7:98028400-98030600	Active TSS	HMEC	breast
15	chr7:98028400-98030800	Active TSS	H1 Cell Line	embryonic stem cell
16	chr7:98028400-98030800	Active TSS	Rectal Mucosa Donor 31	rectum
17	chr7:98028400-98030800	Active TSS	A549	lung
18	chr7:98028600-98030400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr7:98028600-98030400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr7:98028600-98030400	Active TSS	NHEK	skin
21	chr7:98028600-98030800	Active TSS	HepG2	liver
22	chr7:98028600-98030800	Active TSS	K562	blood
23	chr7:98028600-98031000	Active TSS	H9 Cell Line	embryonic stem cell
24	chr7:98028600-98031000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr7:98028600-98031000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr7:98028800-98030800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr7:98028800-98031000	Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr7:98028800-98031000	Active TSS	Breast Myoepithelial Primary Cells	Breast
29	chr7:98029000-98029600	Flanking Active TSS	Liver	Liver
30	chr7:98029000-98029800	Active TSS	Right Atrium	heart
31	chr7:98029000-98030000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr7:98029000-98030000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr7:98029000-98030000	Active TSS	Psoas Muscle	Psoas
34	chr7:98029000-98030200	Active TSS	Fetal Kidney	kidney
35	chr7:98029000-98030600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr7:98029000-98030600	Active TSS	Esophagus	oesophagus
37	chr7:98029000-98030800	Active TSS	Hela-S3	cervix
38	chr7:98029000-98031000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr7:98029200-98029600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr7:98029200-98029600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr7:98029200-98029600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr7:98029200-98029600	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
43	chr7:98029200-98029600	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
44	chr7:98029200-98029600	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
45	chr7:98029200-98029600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
46	chr7:98029200-98029600	Flanking Active TSS	Placenta	Placenta
47	chr7:98029200-98029600	Flanking Active TSS	Left Ventricle	heart
48	chr7:98029200-98029600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
49	chr7:98029200-98029600	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
50	chr7:98029200-98029600	Flanking Active TSS	GM12878-XiMat	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links