Variant report

Variant	esv1803572
Chromosome Location	chr7:3327994-3341589
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:480)
CpG islands
(count:549)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:3340510-3340769	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:3340556-3340788	K562	blood:	n/a	n/a
3	BACH1	chr7:3336841-3337035	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:3339959-3340991	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCLAF1	chr7:3340441-3340719	GM12878	blood:	n/a	chr7:3340634-3340647 chr7:3340524-3340537
6	BCLAF1	chr7:3340395-3340873	GM12878	blood:	n/a	chr7:3340634-3340647 chr7:3340524-3340537 chr7:3340744-3340757
7	BHLHE40	chr7:3340387-3340937	GM12878	blood:	n/a	chr7:3340519-3340535 chr7:3340527-3340543
8	BHLHE40	chr7:3340409-3341002	HepG2	liver:	n/a	chr7:3340932-3340948 chr7:3340519-3340535 chr7:3340527-3340543
9	BHLHE40	chr7:3340404-3341008	K562	blood:	n/a	chr7:3340932-3340948 chr7:3340519-3340535 chr7:3340527-3340543
10	BRCA1	chr7:3340563-3340738	HepG2	liver:	n/a	n/a
11	CBX3	chr7:3340439-3340719	K562	blood:	n/a	n/a
12	CBX3	chr7:3340484-3340710	K562	blood:	n/a	n/a
13	CBX3	chr7:3340323-3340885	HCT-116	colon:	n/a	n/a
14	CCNT2	chr7:3340411-3341005	K562	blood:	n/a	n/a
15	CHD1	chr7:3340292-3340917	IMR90	lung:	n/a	n/a
16	CHD2	chr7:3340511-3340673	HepG2	liver:	n/a	n/a
17	CHD2	chr7:3334435-3334713	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr7:3340606-3340636	K562	blood:	n/a	n/a
19	CHD2	chr7:3340519-3340719	GM12878	blood:	n/a	n/a
20	CHD2	chr7:3340488-3340695	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr7:3339627-3339800	HepG2	liver:	n/a	n/a
22	CREB1	chr7:3340365-3341037	HepG2	liver:	n/a	n/a
23	CREB1	chr7:3340132-3341053	A549	lung:	n/a	n/a
24	CTBP2	chr7:3340345-3341019	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr7:3340580-3340730	HFF-Myc	foreskin:	n/a	n/a
26	CTCF	chr7:3340505-3340757	Medullo	brain:	n/a	n/a
27	CTCF	chr7:3340540-3340690	NB4	blood:	n/a	n/a
28	CTCF	chr7:3340539-3340714	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr7:3340496-3340772	GM10248	blood:	n/a	n/a
30	CTCF	chr7:3340503-3340768	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr7:3340385-3340749	H1-hESC	embryonic stem cell:	n/a	chr7:3340483-3340496
32	CTCF	chr7:3340520-3340670	HCFaa	heart:	n/a	n/a
33	CTCF	chr7:3340410-3340825	K562	blood:	n/a	chr7:3340483-3340496
34	CTCF	chr7:3340540-3340690	GM12875	blood:	n/a	n/a
35	CTCF	chr7:3340418-3340769	T-47D	breast:	n/a	chr7:3340483-3340496
36	CTCF	chr7:3340520-3340670	HRE	kidney:	n/a	n/a
37	CTCF	chr7:3340484-3340725	MCF-7	breast:	n/a	n/a
38	CTCF	chr7:3340460-3340610	GM12868	blood:	n/a	chr7:3340483-3340496
39	CTCF	chr7:3340320-3340470	A549	lung:	n/a	n/a
40	CTCF	chr7:3340560-3340710	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr7:3340560-3340710	AG09319	gingival:	n/a	n/a
42	CTCF	chr7:3341560-3341710	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr7:3340560-3340710	HMEC	breast:	n/a	n/a
44	CTCF	chr7:3340540-3340690	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr7:3340520-3340670	BJ	skin:	n/a	n/a
46	CTCF	chr7:3340540-3340690	NHLF	lung:	n/a	n/a
47	CTCF	chr7:3340580-3340730	GM12867	blood:	n/a	n/a
48	CTCF	chr7:3340540-3340690	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr7:3340310-3340368	GM19238	blood:	n/a	n/a
50	CTCF	chr7:3340456-3340765	Gliobla	brain:	n/a	chr7:3340483-3340496

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3340866-3340916	T-47D	breast:	n/a
2	chr7:3340866-3340916	HepG2	liver:	n/a
3	chr7:3337443-3337493	BE2_C	brain:	n/a
4	chr7:3340866-3340916	Caco-2	colon:	n/a
5	chr7:3338498-3338548	AG04449	skin:	fetal
6	chr7:3338723-3338773	HEEpiC	esophagus:	n/a
7	chr7:3337443-3337493	ovcar-3	ovarian:	n/a
8	chr7:3340866-3340916	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:3341524-3341574	A549	lung:	n/a
10	chr7:3340866-3340916	Hepatocyte	liver:	n/a
11	chr7:3340866-3340916	HCPEpiC	choroid plexus:	n/a
12	chr7:3340866-3340916	H1-hESC	embryonic stem cell:	embryo
13	chr7:3339766-3339816	SK-N-SH	brain:	n/a
14	chr7:3341524-3341574	NT2-D1	testis:	n/a
15	chr7:3340979-3341029	SKMC	muscle:	n/a
16	chr7:3340459-3340509	HUVEC	blood vessel:	n/a
17	chr7:3337443-3337493	HNPCEpiC	eye:	n/a
18	chr7:3337443-3337493	AG04449	skin:	fetal
19	chr7:3340860-3340910	ovcar-3	ovarian:	n/a
20	chr7:3340459-3340509	HRCEpiC	kidney:	n/a
21	chr7:3340860-3340910	HRPEpiC	eye:	n/a
22	chr7:3339766-3339816	PANC-1	pancreas:	n/a
23	chr7:3340860-3340910	NHDF-neo	bronchial:	n/a
24	chr7:3340860-3340910	HRCEpiC	kidney:	n/a
25	chr7:3337443-3337493	HMEC	breast:	n/a
26	chr7:3340459-3340509	BE2_C	brain:	n/a
27	chr7:3338723-3338773	H1-hESC	embryonic stem cell:	embryo
28	chr7:3340860-3340910	GM12878	blood:	n/a
29	chr7:3338723-3338773	HRCEpiC	kidney:	n/a
30	chr7:3340979-3341029	GM12878	blood:	n/a
31	chr7:3341524-3341574	U87	brain:	n/a
32	chr7:3340459-3340509	HCM	heart:	n/a
33	chr7:3341524-3341574	AG04450	lung:	fetal
34	chr7:3340459-3340509	LNCaP	prostate:	n/a
35	chr7:3338723-3338773	Hepatocyte	liver:	n/a
36	chr7:3339766-3339816	AoSMC	blood vessel:	n/a
37	chr7:3339766-3339816	Hepatocyte	liver:	n/a
38	chr7:3337443-3337493	SK-N-SH	brain:	n/a
39	chr7:3338723-3338773	NB4	blood:	n/a
40	chr7:3337443-3337493	MCF10A-Er-Src	breast:	n/a
41	chr7:3340866-3340916	HUVEC	blood vessel:	n/a
42	chr7:3340866-3340916	U87	brain:	n/a
43	chr7:3340979-3341029	AG09309	skin:	n/a
44	chr7:3338723-3338773	IMR90	lung:	fetal
45	chr7:3340860-3340910	AG09319	gingival:	n/a
46	chr7:3340979-3341029	RPTEC	kidney:	n/a
47	chr7:3338723-3338773	HepG2	liver:	n/a
48	chr7:3340979-3341029	HCPEpiC	choroid plexus:	n/a
49	chr7:3337443-3337493	HepG2	liver:	n/a
50	chr7:3340979-3341029	NH-A	brain:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:3250247..3250807-chr7:3340190..3341077,3	MCF-7	breast:
2	chr7:3194510..3195232-chr7:3340158..3340723,2	MCF-7	breast:
3	chr7:3254030..3256348-chr7:3338235..3340171,2	MCF-7	breast:
4	chr7:3339718..3341766-chr7:3458306..3459954,2	K562	blood:
5	chr7:3340063..3340822-chr7:3439252..3440083,5	MCF-7	breast:

No data

Variant related genes	Relation type
SDK1	TF binding region
SDK1	CpG island
ENSG00000211544	chromatin interactions

Extended variants
information (count: 771 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1473658	chr7:3327994-3327995	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544478140	chr7:3328004-3328005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190723677	chr7:3328060-3328061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143197958	chr7:3328068-3328069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540279243	chr7:3328070-3328071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554853799	chr7:3328084-3328085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79899951	chr7:3328098-3328099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73286317	chr7:3328123-3328124	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs568790630	chr7:3328135-3328136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs73286319	chr7:3328140-3328141	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs115419865	chr7:3328155-3328156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550881092	chr7:3328170-3328171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558518384	chr7:3328180-3328181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150921021	chr7:3328223-3328224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576148845	chr7:3328225-3328226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183370313	chr7:3328234-3328235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368806627	chr7:3328236-3328237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373507195	chr7:3328254-3328255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569057033	chr7:3328304-3328305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535831921	chr7:3328309-3328310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1473657	chr7:3328315-3328316	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs576001538	chr7:3328333-3328334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544852010	chr7:3328362-3328363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558173328	chr7:3328388-3328389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs578104432	chr7:3328422-3328423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139457817	chr7:3328425-3328426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559800545	chr7:3328485-3328486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1581564	chr7:3328498-3328499	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs542214334	chr7:3328536-3328537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562184564	chr7:3328543-3328544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs1818932	chr7:3328565-3328566	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs143532858	chr7:3328580-3328581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571470585	chr7:3328586-3328587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527444139	chr7:3328588-3328589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187877794	chr7:3328601-3328602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369241617	chr7:3328602-3328603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566948130	chr7:3328630-3328631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535996837	chr7:3328643-3328644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549510876	chr7:3328649-3328650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569188038	chr7:3328654-3328655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371018931	chr7:3328682-3328683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537877466	chr7:3328713-3328714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558395372	chr7:3328718-3328719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371807538	chr7:3328747-3328748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191526786	chr7:3328750-3328751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534105493	chr7:3328755-3328756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1818931	chr7:3328762-3328763	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs553487676	chr7:3328764-3328765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572132270	chr7:3328783-3328784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs146751439	chr7:3328814-3328815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:432 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3325600-3334400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:3329400-3330200	Enhancers	HSMMtube	muscle
3	chr7:3330200-3330400	Flanking Active TSS	HSMMtube	muscle
4	chr7:3332600-3333200	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr7:3333400-3334800	Enhancers	Duodenum Mucosa	Duodenum
6	chr7:3333600-3334800	Enhancers	H1 Cell Line	embryonic stem cell
7	chr7:3333600-3334800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:3333600-3334800	Enhancers	Fetal Intestine Small	intestine
9	chr7:3334000-3334200	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr7:3334200-3334600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr7:3334200-3334800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr7:3334200-3334800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr7:3334200-3334800	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr7:3334200-3334800	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr7:3334200-3334800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
16	chr7:3334200-3334800	Enhancers	Fetal Intestine Large	intestine
17	chr7:3334200-3334800	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr7:3334400-3334600	Enhancers	Fetal Thymus	thymus
19	chr7:3334400-3334800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr7:3334400-3334800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
21	chr7:3334400-3334800	Enhancers	Pancreas	Pancrea
22	chr7:3334400-3334800	Enhancers	Stomach Mucosa	stomach
23	chr7:3334600-3334800	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr7:3334600-3334800	Enhancers	H9 Cell Line	embryonic stem cell
25	chr7:3334600-3334800	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr7:3334800-3336600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr7:3334800-3336800	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr7:3334800-3337000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr7:3334800-3338400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr7:3334800-3339600	Weak transcription	Pancreas	Pancrea
31	chr7:3335000-3336600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr7:3335000-3340000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr7:3336800-3337000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr7:3336800-3337000	Enhancers	H1 Cell Line	embryonic stem cell
35	chr7:3336800-3337000	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr7:3337000-3337600	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr7:3337000-3338400	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr7:3337600-3339800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr7:3338200-3339000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr7:3338200-3339400	Enhancers	Adipose Nuclei	Adipose
41	chr7:3338400-3338600	Enhancers	H9 Cell Line	embryonic stem cell
42	chr7:3338400-3338600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr7:3338400-3339400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr7:3338600-3338800	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr7:3338600-3339000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr7:3338600-3339600	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr7:3338600-3340200	Enhancers	NHDF-Ad	bronchial
48	chr7:3339000-3339400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr7:3339000-3339800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr7:3339200-3339800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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