Variant report

Variant	nsv599486
Chromosome Location	chr5:116607979-116669707
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	CEBPB	chr5:116628372-116628472	A549	lung:	n/a	n/a
2	CEBPB	chr5:116635780-116636181	MCF-7	breast:	n/a	chr5:116635987-116636004
3	CEBPB	chr5:116642854-116643009	H1-hESC	embryonic stem cell:	n/a	chr5:116642923-116642936 chr5:116642923-116642936 chr5:116642925-116642936
4	CEBPB	chr5:116617917-116618117	HepG2	liver:	n/a	n/a
5	CTCF	chr5:116654360-116654510	Caco-2	colon:	n/a	chr5:116654405-116654418
6	CTCF	chr5:116654340-116654490	HBMEC	blood vessel:	n/a	chr5:116654405-116654418
7	CTCF	chr5:116662840-116662990	GM12864	blood:	n/a	n/a
8	CTCF	chr5:116616000-116616150	MCF-7	breast:	n/a	n/a
9	CTCF	chr5:116662818-116663057	GM12878	blood:	n/a	n/a
10	CTCF	chr5:116654360-116654510	MCF-7	breast:	n/a	chr5:116654405-116654418
11	CTCF	chr5:116662760-116662910	GM12873	blood:	n/a	n/a
12	CTCF	chr5:116654320-116654470	Caco-2	colon:	n/a	chr5:116654405-116654418
13	CTCF	chr5:116654326-116654530	MCF-7	breast:	n/a	chr5:116654405-116654418
14	CTCF	chr5:116662800-116662950	NB4	blood:	n/a	n/a
15	CTCF	chr5:116654360-116654510	HEK293	kidney:	n/a	chr5:116654405-116654418
16	CTCF	chr5:116654260-116654410	HCT-116	colon:	n/a	n/a
17	CTCF	chr5:116654300-116654450	HEEpiC	esophagus:	n/a	chr5:116654405-116654418
18	CTCF	chr5:116654354-116654441	MCF-7	breast:	n/a	chr5:116654405-116654418
19	CTCF	chr5:116662800-116662950	HCT-116	colon:	n/a	n/a
20	CTCF	chr5:116662818-116662954	MCF-7	breast:	n/a	n/a
21	CTCF	chr5:116654360-116654510	GM12869	blood:	n/a	chr5:116654405-116654418
22	CTCF	chr5:116662823-116662964	MCF-7	breast:	n/a	n/a
23	CTCF	chr5:116663020-116663170	BE2_C	brain:	n/a	n/a
24	CTCF	chr5:116654340-116654490	HAc	cerebellar:	n/a	chr5:116654405-116654418
25	CTCF	chr5:116654380-116654530	GM12872	blood:	n/a	chr5:116654405-116654418
26	CTCF	chr5:116654360-116654510	GM12871	blood:	n/a	chr5:116654405-116654418
27	CTCF	chr5:116654320-116654470	GM12865	blood:	n/a	chr5:116654405-116654418
28	CTCF	chr5:116654360-116654510	GM06990	blood:	n/a	chr5:116654405-116654418
29	CTCF	chr5:116654300-116654450	HCT-116	colon:	n/a	chr5:116654405-116654418
30	CTCF	chr5:116654290-116654545	MCF-7	breast:	n/a	chr5:116654405-116654418
31	CTCF	chr5:116654360-116654510	NB4	blood:	n/a	chr5:116654405-116654418
32	CTCF	chr5:116616060-116616210	NHEK	skin:	n/a	n/a
33	CTCF	chr5:116654356-116654474	GM19238	blood:	n/a	chr5:116654405-116654418
34	CTCF	chr5:116662820-116662970	HEK293	kidney:	n/a	n/a
35	CTCF	chr5:116654300-116654450	HBMEC	blood vessel:	n/a	chr5:116654405-116654418
36	CTCF	chr5:116654333-116654500	MCF-7	breast:	n/a	chr5:116654405-116654418
37	CTCF	chr5:116654280-116654430	GM12878	blood:	n/a	chr5:116654405-116654418
38	CTCF	chr5:116654280-116654430	GM12873	blood:	n/a	chr5:116654405-116654418
39	CTCF	chr5:116654360-116654510	GM12864	blood:	n/a	chr5:116654405-116654418
40	CTCF	chr5:116662800-116662950	MCF-7	breast:	n/a	n/a
41	CTCF	chr5:116662733-116663013	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr5:116654285-116654545	GM12878	blood:	n/a	chr5:116654405-116654418
43	CTCF	chr5:116662847-116662969	GM12878	blood:	n/a	n/a
44	CTCF	chr5:116654300-116654450	NHEK	skin:	n/a	chr5:116654405-116654418
45	CTCF	chr5:116654340-116654490	RPTEC	kidney:	n/a	chr5:116654405-116654418
46	CTCF	chr5:116654300-116654450	BE2_C	brain:	n/a	chr5:116654405-116654418
47	CTCF	chr5:116654340-116654490	GM12873	blood:	n/a	chr5:116654405-116654418
48	CTCF	chr5:116662840-116662990	BE2_C	brain:	n/a	n/a
49	CTCF	chr5:116654340-116654490	MCF-7	breast:	n/a	chr5:116654405-116654418
50	CTCF	chr5:116654340-116654490	HMEC	breast:	n/a	chr5:116654405-116654418

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:116640666-116640716	NH-A	brain:	n/a
2	chr5:116640666-116640716	AG09319	gingival:	n/a
3	chr5:116640666-116640716	AG09309	skin:	n/a
4	chr5:116640666-116640716	K562	blood:	n/a
5	chr5:116640666-116640716	HCT-116	colon:	n/a
6	chr5:116640666-116640716	AG04449	skin:	fetal
7	chr5:116640666-116640716	BJ	skin:	n/a
8	chr5:116640666-116640716	CMK	blood:	n/a
9	chr5:116640666-116640716	HRE	kidney:	n/a
10	chr5:116640666-116640716	Hela-S3	cervix:	n/a
11	chr5:116640666-116640716	HepG2	liver:	n/a
12	chr5:116640666-116640716	T-47D	breast:	n/a
13	chr5:116640666-116640716	NT2-D1	testis:	n/a
14	chr5:116640666-116640716	IMR90	lung:	fetal
15	chr5:116640666-116640716	U87	brain:	n/a
16	chr5:116640666-116640716	HUVEC	blood vessel:	n/a
17	chr5:116640666-116640716	HIPEpiC	eye:	n/a
18	chr5:116640666-116640716	RPTEC	kidney:	n/a
19	chr5:116640666-116640716	HAEpiC	amniotic membrane:	n/a
20	chr5:116640666-116640716	HCF	heart:	n/a
21	chr5:116640666-116640716	HEK293	kidney:	embryo
22	chr5:116640666-116640716	BE2_C	brain:	n/a
23	chr5:116640666-116640716	NHBE	bronchial:	n/a
24	chr5:116640666-116640716	LNCaP	prostate:	n/a
25	chr5:116640666-116640716	SAEC	small airway:	n/a
26	chr5:116640666-116640716	SK-N-SH	brain:	n/a
27	chr5:116640666-116640716	ovcar-3	ovarian:	n/a
28	chr5:116640666-116640716	Hepatocyte	liver:	n/a
29	chr5:116640666-116640716	NHDF-neo	bronchial:	n/a
30	chr5:116640666-116640716	HMEC	breast:	n/a
31	chr5:116640666-116640716	H1-hESC	embryonic stem cell:	embryo
32	chr5:116640666-116640716	Jurkat	blood:	n/a
33	chr5:116640666-116640716	GM12878	blood:	n/a
34	chr5:116640666-116640716	GM12891	blood:	n/a
35	chr5:116640666-116640716	GM06990	blood:	n/a
36	chr5:116640666-116640716	A549	lung:	n/a
37	chr5:116640666-116640716	SKMC	muscle:	n/a
38	chr5:116640666-116640716	SK-N-MC	brain:	n/a
39	chr5:116640666-116640716	HPAEpiC	pulmonary alveolar:	n/a
40	chr5:116640666-116640716	GM12892	blood:	n/a
41	chr5:116640666-116640716	ProgFib	skin:	n/a
42	chr5:116640666-116640716	MCF10A-Er-Src	breast:	n/a
43	chr5:116640666-116640716	HRPEpiC	eye:	n/a
44	chr5:116640666-116640716	AoSMC	blood vessel:	n/a
45	chr5:116640666-116640716	AG10803	skin:	n/a
46	chr5:116640666-116640716	PFSK-1	brain:	n/a
47	chr5:116640666-116640716	HCM	heart:	n/a
48	chr5:116640666-116640716	HL-60	blood:	n/a
49	chr5:116640666-116640716	Caco-2	colon:	n/a
50	chr5:116640666-116640716	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:54966032..54966839-chr5:116662215..116662871,2	MCF-7	breast:
2	chr5:116648124..116649695-chr5:116650114..116652832,2	MCF-7	breast:
3	chr5:116654194..116654786-chr5:116790174..116790911,2	MCF-7	breast:
4	chr5:116640598..116642872-chr5:116653886..116656099,2	MCF-7	breast:
5	chr5:116649673..116651747-chr5:116653579..116656311,3	MCF-7	breast:
6	chr5:116649673..116651747-chr5:116653579..116656311,3	MCF-7	breast:
7	chr5:116648124..116649695-chr5:116650114..116652832,2	MCF-7	breast:
8	chr5:116640598..116642872-chr5:116653886..116656099,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEMA6A-9	chr5:116636800-116637138	NONHSAT103385

Variant related genes	Relation type
RPL35AP15	TF binding region
RPL35AP15	CpG island

Extended variants
information (count: 938 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:938 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6595026	chr5:116607979-116607980	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs544280555	chr5:116607991-116607992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183697425	chr5:116608008-116608009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564171138	chr5:116608020-116608021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139282678	chr5:116608026-116608027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546614370	chr5:116608027-116608028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188208788	chr5:116608050-116608051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs111931646	chr5:116608074-116608075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs35234858	chr5:116608075-116608076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551977589	chr5:116608078-116608079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34613725	chr5:116608080-116608081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs10630467	chr5:116608081-116608082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576220038	chr5:116608103-116608104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs79406160	chr5:116608108-116608109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569071540	chr5:116608109-116608110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs538052012	chr5:116608146-116608147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144209260	chr5:116608159-116608160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571754263	chr5:116608163-116608164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146050542	chr5:116608177-116608178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs6874362	chr5:116608179-116608180	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs72812534	chr5:116608188-116608189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs535712127	chr5:116608199-116608200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541029503	chr5:116608203-116608204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs75787201	chr5:116608242-116608243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140193310	chr5:116608272-116608273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs13183048	chr5:116608286-116608287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs193267648	chr5:116608295-116608296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs77301304	chr5:116608305-116608306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577700260	chr5:116608346-116608347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574036535	chr5:116608376-116608377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201448198	chr5:116608438-116608439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370251733	chr5:116608439-116608440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560061666	chr5:116608448-116608449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs143930546	chr5:116608476-116608477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373094250	chr5:116608490-116608491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542866517	chr5:116608534-116608535	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562892356	chr5:116608536-116608537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531780266	chr5:116608538-116608539	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185443911	chr5:116608542-116608543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556687244	chr5:116608584-116608585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113307406	chr5:116608599-116608600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527757143	chr5:116608632-116608633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148991374	chr5:116608638-116608639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567609166	chr5:116608691-116608692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs142920892	chr5:116608710-116608711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116565305	chr5:116608724-116608725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569212576	chr5:116608755-116608756	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544857031	chr5:116608782-116608783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs13184380	chr5:116608841-116608842	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs557907772	chr5:116608847-116608848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116606600-116610000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:116607000-116608800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:116607600-116608400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:116608400-116609600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:116608800-116609400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr5:116609400-116609600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:116609400-116609800	Enhancers	Stomach Mucosa	stomach
8	chr5:116609600-116609800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:116617400-116617600	ZNF genes & repeats	Pancreas	Pancrea
10	chr5:116622200-116622400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr5:116622400-116622800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr5:116622400-116623200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:116622400-116623400	Enhancers	Fetal Heart	heart
14	chr5:116623400-116624200	Weak transcription	Fetal Heart	heart
15	chr5:116624200-116624400	Enhancers	Fetal Heart	heart
16	chr5:116625800-116626400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:116626000-116626200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr5:116631200-116634600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr5:116631800-116633600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr5:116632600-116633400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr5:116632600-116633600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr5:116632600-116633600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr5:116632600-116633600	Enhancers	Colon Smooth Muscle	Colon
24	chr5:116632600-116634200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr5:116632600-116636200	Enhancers	Fetal Heart	heart
26	chr5:116632800-116633000	Enhancers	Fetal Stomach	stomach
27	chr5:116632800-116633200	Enhancers	Stomach Smooth Muscle	stomach
28	chr5:116632800-116633600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr5:116632800-116633600	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr5:116632800-116636000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr5:116633000-116634000	Weak transcription	Fetal Stomach	stomach
32	chr5:116633200-116633600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr5:116633200-116633600	Enhancers	Fetal Kidney	kidney
34	chr5:116633200-116635000	Weak transcription	Stomach Smooth Muscle	stomach
35	chr5:116633400-116634200	Enhancers	Primary hematopoietic stem cells	blood
36	chr5:116633400-116634600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr5:116633400-116638400	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr5:116633600-116634000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr5:116633600-116634200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr5:116633600-116634800	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr5:116633600-116635000	Weak transcription	Colon Smooth Muscle	Colon
42	chr5:116633600-116638600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr5:116633600-116638600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr5:116634000-116634200	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr5:116634000-116634200	Enhancers	Fetal Lung	lung
46	chr5:116634000-116635600	Enhancers	Fetal Stomach	stomach
47	chr5:116634200-116636400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr5:116634200-116637000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr5:116634200-116638600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr5:116634400-116635400	Weak transcription	Fetal Lung	lung

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